{"title":"聚合物在低温/室温下实现自愈的要求","authors":"Kanyarat Mantala, Daniel Crespy","doi":"10.1021/acs.macromol.5c01424","DOIUrl":null,"url":null,"abstract":"Low-temperature self-healing polymers are crucial, as many real-world damage events occur in environments where external heating is impractical or energy-inefficient. However, achieving effective self-healing at these temperatures remains a significant challenge due to the restricted polymer chain mobility. To tackle this challenge, strategies have been investigated, such as modulating the strength of reversible chemical bonds; however, these approaches alone are often inadequate. In this Perspective, we comprehensively examine the factors influencing polymer chain mobility under low and ambient temperatures. We focus on optimizing material design to balance mechanical strength and healing performance, considering factors such as polymers with low glass transition temperatures, different types of polymers, branched to hyperbranched architectures, the role of shape-memory effects, and the facilitative impact of solvents. These insights provide a foundation for designing self-healing polymers tailored to specific application demands. Furthermore, we outline key considerations in synthetic design, molecular mobility, healing time, mechanical properties, and other functional properties, such as hydrophobicity and impedance modulus, as well as perspectives for creating materials that effectively self-heal at low or room temperatures.","PeriodicalId":51,"journal":{"name":"Macromolecules","volume":"338 1","pages":""},"PeriodicalIF":5.2000,"publicationDate":"2025-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Requirements for Achieving Self-Healing at Low/Room Temperature in Polymers\",\"authors\":\"Kanyarat Mantala, Daniel Crespy\",\"doi\":\"10.1021/acs.macromol.5c01424\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Low-temperature self-healing polymers are crucial, as many real-world damage events occur in environments where external heating is impractical or energy-inefficient. However, achieving effective self-healing at these temperatures remains a significant challenge due to the restricted polymer chain mobility. To tackle this challenge, strategies have been investigated, such as modulating the strength of reversible chemical bonds; however, these approaches alone are often inadequate. In this Perspective, we comprehensively examine the factors influencing polymer chain mobility under low and ambient temperatures. We focus on optimizing material design to balance mechanical strength and healing performance, considering factors such as polymers with low glass transition temperatures, different types of polymers, branched to hyperbranched architectures, the role of shape-memory effects, and the facilitative impact of solvents. These insights provide a foundation for designing self-healing polymers tailored to specific application demands. Furthermore, we outline key considerations in synthetic design, molecular mobility, healing time, mechanical properties, and other functional properties, such as hydrophobicity and impedance modulus, as well as perspectives for creating materials that effectively self-heal at low or room temperatures.\",\"PeriodicalId\":51,\"journal\":{\"name\":\"Macromolecules\",\"volume\":\"338 1\",\"pages\":\"\"},\"PeriodicalIF\":5.2000,\"publicationDate\":\"2025-10-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Macromolecules\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.macromol.5c01424\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecules","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.macromol.5c01424","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Requirements for Achieving Self-Healing at Low/Room Temperature in Polymers
Low-temperature self-healing polymers are crucial, as many real-world damage events occur in environments where external heating is impractical or energy-inefficient. However, achieving effective self-healing at these temperatures remains a significant challenge due to the restricted polymer chain mobility. To tackle this challenge, strategies have been investigated, such as modulating the strength of reversible chemical bonds; however, these approaches alone are often inadequate. In this Perspective, we comprehensively examine the factors influencing polymer chain mobility under low and ambient temperatures. We focus on optimizing material design to balance mechanical strength and healing performance, considering factors such as polymers with low glass transition temperatures, different types of polymers, branched to hyperbranched architectures, the role of shape-memory effects, and the facilitative impact of solvents. These insights provide a foundation for designing self-healing polymers tailored to specific application demands. Furthermore, we outline key considerations in synthetic design, molecular mobility, healing time, mechanical properties, and other functional properties, such as hydrophobicity and impedance modulus, as well as perspectives for creating materials that effectively self-heal at low or room temperatures.
期刊介绍:
Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.